Nova H R
J Neurosurg. 1979 Dec;51(6):862-5. doi: 10.3171/jns.1979.51.6.0862.
This report deals with a family in which the maternal grandmother, the mother, and all three male children have port-wine nevi and mega cisterna magna. Two of the three male children have, in addition, congenital communicating hydrocephalus associated with agenesis of the posterior cerebellar vermis. This case of familial communicating hydrocephalus, posterior cerebellar vermis agenesis, port-wine nevus, and mega cisterna magna represents a new neurocutaneous syndrome, possibly transmitted as an autosomal dominant.
本报告涉及一个家族,其中外祖母、母亲以及所有三个男性儿童均患有葡萄酒色斑痣和大枕大池。此外,三个男性儿童中有两个患有先天性交通性脑积水,伴有小脑后蚓部发育不全。这种家族性交通性脑积水、小脑后蚓部发育不全、葡萄酒色斑痣和大枕大池的病例代表了一种新的神经皮肤综合征,可能以常染色体显性方式遗传。